Influence of Recycled Concrete Fine Powder on Durability of Cement Mortar

In this paper,the durability of cement mortar prepared with a recycled-concrete fine powder(RFP)was examined;including the analysis of a variety of aspects,such as the carbonization,sulfate attack and chloride ion erosion resistance.The results indicate that the influence of RFP on these three aspects is different.The carbonization depth after 30 days and the chloride diffusion coefficient of mortar containing 10%RFP decreased by 13.3%and 28.19%.With a further increase in the RFP content,interconnected pores formed between the RFP particles,leading to an acceleration of the penetration rate of CO_(2)and Cl^(−).When the RFP content was less than 50%,the corrosion resistance coefficient of the compressive strength of the mortar was 0.84-1.05 after 90 days of sulfate attack.But the expansion and cracking of the mortar was effectively alleviated due to decrease of the gypsum production.Scanning electron microscope(SEM)analysis has confirmed that 10%RFP contributes to the formation of a dense microstructure in the cement mortar.

Experimental investigation on micro-dynamic behavior of gas explosion suppression with SiO_2 fine powders

To study the effect of inert dust on gas explosion suppression mechanism,SiO_2 fine powders were sprayed to suppress premixed CH_4-Air gas explosion in a 20 L spherical experimental system.In the experiment,high speed schlieren image system was adopted to record explosion flame propagation behaviors,meanwhile,pressure transducers and ion current probes were used to clearly record the explosion flame dynamic characteristics.The experimental results show that the SiO_2 fine powders suppressed evidently the gas explosion flame,and reduced the peak value of pressure and flame speed by more than 40%.The ion current result shows that the SiO_2 super fine powders were easy to contact with and absorb free radicals near the combustion reaction region,which greatly reduced the combustion reaction intensity,and in turn influenced the flame propagation and pressure rising.

Effects of Curing Systems on Properties of High Volume Fine Mineral Powder RPC and Appearance of Hydrates

The effects of different curing systems on the properties of high volume fine mineral powder RPC （reactive powder concrete） and the appearances of hydrates were studied. The experimental results show that dry-heating curing promotes the development of pozzolanic reactivity of fine mineral powder; due to low cement content, 0.20 water-bind ratio and high reactive fine mineral powder content, the strength of RPC increases by around 200% after steam curing and subsequent dry-heating curing. Scanning electron microscopy and energy spectrum diagram showed that： after the high volume fine mineral powder RPC with 0.16 water-bind ratio underwent steam curing and dry-heating curing, there was no significant change in the appearance of hydrates; after the RPC with 0.20 water-bind ratio, the cement content of 150 kg/m3 and more steel slag powder underwent dry-heating curing, there was a certain change in the appearance of C-S-H, the structure of gel was more compact and was uniformly distributed, and the Ca/Si of C-S-H gel decreased from 1.41 to around 1.20.

Influence of MnO_2 Mineralizer on the Crystal Structure,Properties of SiC Kiln Furniture Bonded with Fine Silicon Powder

The properties of SiC kiln furniture bonded with fine silicon powderare related to the bonder’s crystal structure. At high temperature, it will crystallize ina-cristobalite with great bulk effect. MnO2 mineralizer can make a-cristobalite convertto a-tridymite whose bulk effect is small. The crystal structure and its amount were investigated with XRD technique. The influence of different amounts of MnO2 on thecrystal structure and polycrystal transformation, and that of crystal structure on theproperties of kiln furniture were studied. The best proportion of MnO2 added was determined to be 2.0%.

Optimal Conditions for Preparing Ultra-Fine CeO_2 Powders in A Submerged Circulative Impinging Stream Reactor

Cerium carbonate powders were produced in a submerged circulation impinging stream reactor （SCISR） from Ce（NO3）3· 6H2O. NH4HCO3 was used as a precipitant in the reaction. Cerium carbonate powders were roasted to produce ultra-fine cerium dioxide （CeO2） powders. The optimal conditions of such production process were obtained by orthogonal and one-factor experiments. The results showed that ultra-fine and narrowly distributed cerium carbonate powders were produced under the optimal flowing conditions. The concentrations of Ce（NO3）3 and NH4HCO3 solutions were 02,5 and 0.3 mol · L^-1, respectively. The concentration of PEG4000 added in these two solutions was 4 g · L^-1. The stirring ratio, reaction temperature, feeding time, solution pH, reaction time and digestion time were 900 r · min^- 1,80 ℃, 20 min, 5 - 6, 5 min and 1 h, respectively. The final product, CeO2 powders, was obtained by roasting the produced cerium carbonate in air for 3 h at 500 ℃. The finally produced CeO2 powders were torispherical particles with a narrow size distribution of 0.8 -2.5 μm. The crystal structure of CeO2 powders belonged to cubic crystal system and its space point 5 group was OH^5-FM3M. Under optimal conditions, powders produced by SCISR were finer and more narrowly distributed than that by Stirred Tank Reactor （STR）.

DYNAMIC RHEOLOGICAL BEHAVIOR OF POLYPROPYLENE FILLED WITH ULTRA-FINE POWDERED RUBBER PARTICLES

Dynamic rheological characteristics of polypropylene (PP) filled with ultra-fine full-vulcanized powdered rubber (UFPR) composed of styrene-butadiene copolymer were studied through dynamic rheological measurements on an Advanced Rheometric Expansion System (ARES). A specific viscoelastic phenomenon, i.e. 'the second plateau', appeared at low frequencies, and exhibits a certain dependence on the amount of rubber particles and the dispersion state in the matrix. This phenomenon is attributed to the formation of aggregation structure of rubber particles. The analyses of Cole-Cole diagrams of the dynamic viscoelastic functions suggest that the heterogeneity of the composites is enhanced on increasing both particle content and temperature.

An improved sodium silicate binder modified by ultra-fine powder materials

This paper presents a new method of modifying sodium silicate binder with ultra-fine powders. The sodium silicate binder modified by ultra-fine powder A and the organic B can reduce the addition amount of the binder. The results indicate that the 24 h strength has increased by 39.9% at room temperature and the residual strength has decreased by 30.7% at 800℃, compared to the conventional sodium silicate. An available material to improve the moisture resistance was also found by adding about 2% more inorganic C, and it can increase the moist strength by 20%. In the end, the microanalyses are given to explain the modifying machanism, i. e., the ultra-fine powder A can refine the sodium silicate binder to avoid holes in the binder bond, which can increase the 24 h strength at room temperture, and can lead to more cracks in the bond after the molding sand is heated to 800℃. This is because of the stress caused by the new eutectic complex of modified sodium silicate binder.

Hydrogen Reduction:A Novel Method of Synthesizing Ultra-fine Chromic Oxide Powder

The ultra-fine chromic oxide powder was prepared by a novel gas-solid reduction reaction.Na2CrO4 was firstly reduced with hydrogen at 400-600 ℃.The obtained reduction products,mainly the mixture of NaCrO2 and sodium hydroxide（NaOH）,were converted into chromic oxide through hydrolysis followed by calcination.The obtained chromic oxide product was characterized by powder X-ray diffraction（XRD） and SEM.The results show that the hydrolysis process of sodium chromite is the key step and lower reduction temperature helps intensify the hydrolysis process.

Preparation of Ultrafine Tungsten Powder by Sol-Gel Method

Sol-gel method was employed for the preparation of nanoscale tungsten powder. The effects of different preparation conditions on particle size were discussed and the optimum preparation condition was found. The products were characterized by X-ray diffraction, scan electron microscopy and so on. The results show that the intermediate is monoclinic WO3, its particle shape is approximately spherical, and the particle size distribution is narrow. The average particle size is about 60 nm. After deoxidization, WO3 turns into cubic tungsten powder with small particle size （average particle size about 120 nm） and narrow size distribution.

Strengthening of HT250 by modified ultra-fine ceramic powders

In this study, three kinds of modified ultra-fine ceramic powders marked A, B and C, which were prepared by each of three different modifiers mixing with a commercial SiC, were added to HT250 cast iron, respectively, and the effects of the modified ultra-fine ceramic powders on microstructure, mechanical properties and wear resistance were studied. Metallographic examination, tensile test, scanning electron microscopy, and three-dimensional surface topography were applied to analyze and compare the samples containing modified powder with the original samples. The results showed that the most obvious modification effect among the powders was seen in the sample containing powder A, with the graphite and eutectic cells being refined, the tensile strength being increased by 36.9%, and the wear resistance being improved by 45.5% and 47.2% under loads of 150 N and 300 N, respectively. The improvements of mechanical properties and wear resistance in the HT250 cast iron with the modified ultra-fine ceramic powders were attributed to the synergistic effect of the grain refinement with the powder acting as a hard particle phase and the lubrication by the graphite.

Influence and Characterization of Acidity on Fine Silicon Powder Immobilized Photocatalyst

TiO2 photocatalyst was supported with tetrabutyl titanate sol as precursor and fine silicon powder obtained from ferroalloys factory as carder to discuss the influence of pH value of gel precursor on microstructure and activity of photocatalyst in the process of synthesizing nano-TiO2 by using sol-gel method, the purpose of which is to provide fundamental data for the recycle of photocatalytic material. Under the irradiation of ultraviolet light, the photocatalytic degradation rate of methyl orange solution was used to characterize the photocatalytic activity of the sample. The specific surface area of the sample was tested by N2 desorption method, crystal form of TiO2 was analyzed by X-ray powder diffraction, and the microtopography of the sample was observed by scanning electron microscopy. The experimental results showed that the acidity of gel precursor could greatly affect the specific surface area and photocatalytic activity of the photocatalyst, and the optimum pH value of the precursor was determined as 2.0, and at this time the specific surface area of photocatalyst could reach 34.0 m^2/g. In the sample, the proporticn of anatase to rutile is 7：3, which makes l0 mg·L^-1 methyl orange solution fade after irradiation by 15W ultraviolet light for 24 h, and the degradation rate might be up to 98.1%.

AGGREGATE STRUCTURE OF FINE POWDER AND COMPACTION PROCESS

Compacting process of fine powder is greatly affected by the aggregate structure of particles. According to the experiment in which several kinds of silicon nitrides in different partical shape and size were compacted in uniaxialorientation, it is found that the volume compacting rate offorming body differs with the pressure. The aggregatestructure of each sample A, B or C was estimated by applying Cooper's equation to the analysis of the compacting process of each sample

Studies on Acid Leaching Methods for Fine Metal Powder Production

Two different processes (i) alloying followed by selective leaching of alloying constituent and (ii) controlled chemical attack of oversize powder stock were studied in some detail to assess their suitability for metal powder production. In a typical series of experiments on the alloying process, titanium, zirconium and nickel were alloyed with aluminium. The sample was then leached out with acid to yield the metals in powder form. The metal powders generally had a particle size spread in the range of <5 μm. The acid concentration and contact time were varied and both have influences on particle size of the final product. In the second process involving chemical attack of coarse powder, it is shown by taking the example of nickel that a range of particle size could be generated through close control of acid concentration and contact time.

Comparative Study on Super Fine Mesophase Powder and MCMB Used to Manufacture High-Density Isotropic Carbon Bulks

Mesocarbon microbeads （MCMB） and super fine mesophase powder （SFMP） were prepared firstly from a coal tar pitch and then hot-condensed into high-density isotropic carbon （HDIC） bulks under 160 MPa and finally sintered at 1 000 ℃. By analyzing the thermogravimetric behavior of the MCMB and SFMP powders, their volume shrinkage and weight loss during sintering and the bulk density and flexural strengths of their sintered bulks, it was found that the smaller sizes and the richer β-resin contents of SFMP ha）re facilitated formation of sintered bulks with more compact isotropic structure and higher flexural strengths than MCMB. Because of the filling and bonding effects of SFMP on MCMB bulks, addition of SFMP, albeit a little, can greatly increase the flexural strengths of sintered bulks of MCMB. However, adding MCMB, even a slight amount, into SFMP can severely impair the flexural strength of sintered bulks. This might be attributed to both the crack initiation along the boundaries between MCMB and SFMP and the formation of layered texture of MCMB sphere.

Preparation of Strontium Bismuth Tantalum (SBT) Fine Powder by Sol-Gel Process Using Bismuth Subnitrate as Bismuth Source

Strontium bismuth tantalum (SBT) fine power was prepared by Sol-Gel method. Pentaethoxy tantalum, strontium acetate and bismuth subnitrate were used as raw materials, and were dissolved in proper order in ethylene glycol to form transparent sol. The mixed precursor was dried at 80℃ and annealed at 800℃ for 1 h. Crystallized nanometer sized SBT fine powder was obtained and characterized by XRD.

Three Techniques Used to Produce BaTiO₃Fine Powder

Homogeneous BaTiO3 fine powder has been synthesized at (80°C) by using three different chemical methods using the roots TiCl4, BaCl2 and NaOH or Oxalic acid. The resultant powders were characterized using x-ray diffraction (XRD) to estimate the crystal structure, lattice parameters and the crystallite size to investigate the favor method in producing BaTiO3 fine powder. The criteria that was dependent on considering the favor method that was given better results of XRD and demand a least time in preparation which tend to consume a lowest energy.

Preparation of Ultra-fine Salbutamol Sulfate Particles by Reactive Precipitation and Characterization of Dry Powder Inhalant

salbutamol 硫酸盐(SS ) 的极其细小的粒子的准备与一条反应降水小径， salbutamol 和硫的酸与乙醇的溶剂在被用作反应物被完成。粒子的尺寸上的硫的酸集中，反应温度，激动人心的率，和反应时间的效果被调查。二进制混合物乳糖创作了， SS 被准备评估 SS。结果证明有控制直径在 3 渭 m 和 0.8 渭 m 之间变化并且与狭窄的分布的极其细小的 SS 粒子能被完成。由打的粒子组成的形态学成功地被获得。粒子的纯净上面与紫外察觉到达了 98% 。干燥粉末吸入的剂量被与重新使结晶的乳糖混合粒子获得，它充当了一个搬运人。在呼吸道的药的免职数量用一台成双的 impinger 仪器被估计。与 Shapuer 粉末相比(在市场上购买了) ，结果证明 SS 粒子把更多的数量在模拟的肺减退了。

Influence of Recycling Waste Glass as Fine Aggregate on the Concrete Properties

Recent years have witnessed an increase in the quantity of waste glass(WG)across the globe.Replacing the fine aggregate with WG is one of the steps toward preserving the natural resources of the environment and creating low-cost concrete.The present study is concerned with replacing fine aggregates with glass powder(GP)at(0%,15%,30%,and 50%).It has studied the fresh and hardened properties(compressive strength,tensile strength,hardened density,and slump)for all the mentioned percent replacements.The findings have shown that all mixtures containing GP gave acceptable slump results within the design limits(2–5 cm)according to ACI standard 211.1.It has been observed that increasing the proportion of GP led to a decrease in the weight of concrete.Lastly,replacing GP with sand by 30%has led to an increase in the compressive strength by about 2.4%and 12.45%,and the tensile strength by about 2.5%and 26.54%at 7-and 28-d,respectively in comparison to normal concrete.

Microstructure and properties of liquid-phase sintered tungsten heavy alloys by using ultra-fine tungsten powders

The microstructure and properties of liquid-phase sintered 93W-4.9Ni-2.1Fe tungsten heavy alloys using ultra-fine tungsten powders (medium particle size of 700 nm) and original tungsten powders (medium particle size of 3 μm) were investigated respectively. Commercial tungsten powders (original tungsten powders) were mechanically milled in a high-energy attritor mill for 35 h. Ultra-fine tungsten powders and commercial Ni, Fe powders were consolidated into green compacts by using CIP method and liquid-phase sintering at 1 465 ℃ for 30 min in the dissociated ammonia atmosphere. Liquid-phase sintered tungsten heavy alloys using ultra-fine tungsten powders exhibit full densification (above 99% in relative density) and higher strength and elongation compared with conventional liquid-phase sintered alloys using original tungsten powders due to lower sintering temperature at 1 465 ℃ and short sintering time. The mechanical properties of sintered tungsten heavy alloy are found to be mainly dependent on the particles size of raw tungsten powders and liquid-phase sintering temperature.

Crystal Structure of Ba_xSr_1-xTiO₃Fine Powder

Various compositions of the system BaxSr1-xTiO3 (BST) have been elaborated both as fine powders and ceramic monoliths, using the co-precipitation route within a warmed supersaturated solution of oxalic acid. The appropriate stoichiometry was determined from the mixtures of precisely titrated aqueous solutions of cations chlorides (SrCl2, BaCl2, and TiCl4). The reason of this process was to apply low sintering temperature in production of BST samples with ultra-fine powders. These powders primarily calcined at (850°C) for (5 hr) were used to elaborate ceramics after pellets sintering at (1200°C) during (8 hrs). Indeed, XRD patterns were confirmed that the samples are a pure phase and a perovskite cubic structural type at (x = 0, 0.5, 0.6). Whereas, (x = 0.7, 0.8, 0.9, 1) showed a tetragonal phase. There is agreement between the FTIR and XRD analysis, by the relation of the wave vector (K) and lattice constant. It was deduced a stimulated relation between (x) and (K). The results of TEM, they were clear that the lowest particle sizes investigated of BST powders nearly (36 - 50 nm).